What Covary does and how to think about the results
Covary is designed for alignment-free, translation-aware comparison of DNA sequence records. It helps users explore relationships among sequences through embeddings, distances, dendrograms, and downloadable result files.
1. Input
Covary accepts multi-FASTA input. Each FASTA record should have one header and one DNA sequence. Headers become the labels used in plots, tables, dendrograms, downloaded TSV files, and shared result pages.
- Use simple, meaningful headers such as
>speciesA_geneX_sample01. - Keep records biologically comparable when possible, such as the same marker, gene, locus, region, or genome scope.
- Avoid hidden web-page downloads. URL analysis should point to raw FASTA text.
2. Analysis
Covary cleans and encodes records, generates machine-learning-derived embeddings, reduces the representation into PCA, t-SNE, and UMAP spaces, calculates pairwise distances, and reconstructs hierarchical relationships.
3. Results
The Results viewer shows embeddings, dendrograms, sequence statistics, analytics, raw downloads, experiment context, sharing controls, and coalescence analysis when the available result payload supports it.
Very large outputs may be capped in the server-served viewer to protect browser and server memory. When a section is capped, download the raw TSV files and use Browser Visualizer to explore them locally.
4. Browser Visualizer
Browser Visualizer is a Pro feature for local-only exploration of downloaded TSV files. Files are loaded in your browser and are not sent back to the web server or compute resources.
- Use embedding TSVs to render PCA, t-SNE, or UMAP scatter plots.
- Use distance TSVs to render heatmaps, distance summaries, analytics, and coalescence outputs.
- Use it when server-served heatmaps or analytics are capped because the run is large.
5. Coalescence Analysis
Coalescence Analysis reconstructs sample-level closeness from repeated label patterns. For headers like marker1_sampleA and marker2_sampleA, Covary can group by marker and sample to infer how samples relate cumulatively across markers.
This does not re-read the original DNA sequence; it uses Covary-derived distances among labeled records. It is useful when several markers, loci, or partitions represent the same sample set.
6. Sharing and context
Shared results are easier to understand when the experiment context is filled in. Add objectives, background, sample information, preprocessing notes, and interpretation notes before sending a public link to collaborators.
For Free and Institutional users, new analyses are public by default unless changed. Pro runs are private by default.